二甲基亚砜
细胞毒性
溶剂
化学
毒性
兴奋
活力测定
细胞毒性T细胞
β淀粉样蛋白
生物化学
淀粉样蛋白(真菌学)
药理学
溶剂效应
溶剂暴露
生物物理学
细胞
体外
有机化学
肽
氧化应激
生物
无机化学
作者
Yanhong Fu,Jiafa Zhang,Canhong Yang,Yuanyuan Wang,Yunzhu Yang,Pingming Qiu,Wei‐Bing Xie,Shufen Zhang,Tianming Lǚ
标识
DOI:10.1177/10915818251338235
摘要
Dimethyl sulfoxide (DMSO) is commonly used as a solvent for preparing amyloid-beta (Aβ) peptides implicated in Alzheimer’s disease. While considered relatively non-toxic at low concentrations, DMSO itself may exert biological effects that could confound experimental outcomes, especially for weakly cytotoxic substances like Aβ. Seven brain cell types (BV-2, N2a, SH-SY5Y, U87, neurons, astrocytes, microglia) were treated with varying DMSO concentrations or Aβ1-42 oligomers/protofibrils/fibrils prepared using DMSO. Cell viability was assessed by CCK-8 and LDH assays. Matched DMSO controls were prepared alongside Aβ treatments to delineate solvent effects. Low DMSO concentrations (0.0625-0.015625%) exhibited hormetic cytoprotective and growth-promoting effects, while higher concentrations (≥2%) were cytotoxic. Importantly, these hormetic solvent effects confounded the measurement of Aβ cytotoxicity. By accounting for matched DMSO controls, the study revealed that Aβ fibril toxicity may have been underestimated due to the cytoprotective solvent effects of low DMSO concentrations used in their preparation. In conclusion, DMSO exhibits complex hormetic dose-responses that can significantly influence experimental outcomes, especially for weakly cytotoxic agents like Aβ. Rigorous solvent controls are crucial to delineate genuine substance effects from potential solvent confounds and avoid erroneous interpretations.
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